Clinical Trial

Medical Adhesive and Barrier Products for Preventing MARSI in Central Venous Catheter Dressings

Recruiting
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Summary
The goal of this clinical trial is to compare three different dressing securement strategies used for central venous catheters (CVCs) to determine which is more effective in preventing medical adhesive-related skin injury (MARSI) among adults admitted to a Chest Diseases Intensive Care Unit. The main questions it aims to answer are: Does the type of dressing securement affect the occurrence of MARSI? Which dressing securement strategy is most effective in preventing CVC-related MARSI? Researchers will compare: acrylic adhesive tape, silicone adhesive tape, and barrier film combined with acrylic adhesive tape to determine which dressing securement strategy provides the best protection against CVC-related MARSI. Participants will: be randomly assigned to one of the three dressing securement strategies, receive the assigned dressing securement throughout the study period, undergo regular skin assessments for signs of MARSI, and be followed for up to 21 days or until catheter removal.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-07-05.
Trial Details
NCT Number NCT07697430
Lead Sponsor Azize Özdaş Gündoğan
Conditions Medical Adhesive Related Skin Injury, Central Venous Catheter
Enrollment 162 participants
Start Date 2026-06-01
Primary Completion 2027-06-01 (estimated)
Study Completion 2027-06-01 (estimated)
Updated on ClinicalTrials.gov 2026-07-21